Výsledky vyhledávání - "Hendriks, J.J.E."

Increased cytokines, chemokines and soluble adhesion molecules in exhaled breath condensate of asthmatic children

Autor: Robroeks, C.M., Rijkers, G.T., Jöbsis, Q., Hendriks, J.J.E., Damoiseaux, J.G.M.C., Zimmermann, L.J.I., van Schayck, O.P., Dompeling, E.D.

Publikováno v: Clinical and Experimental Allergy, 40(1), 77-84. Wiley-Blackwell

BACKGROUND: Airway inflammation in asthma is characterized by the production of cytokines, chemokines and soluble adhesion molecules. The assessment of these inflammatory biomarkers in exhaled breath condensate (EBC) is hampered by low detection rate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::2b5ff58d5f208935c1c03d51ee3162b0
https://cris.maastrichtuniversity.nl/en/publications/17031ac7-7554-4876-a4ab-5f45b681545c

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Structural lung changes, lung function and non-invasive inflammatory markers in cystic fibrosis

Autor: Robroeks, C.M., Roozeboom, M.H., de Jong, P.A., Tiddens, H.A., Jöbsis, Q., Hendriks, J.J.E., Yntema, J.B., Brackel, H.L., van Gent, R., Robben, S., Dompeling, E.D.

Publikováno v: Pediatric Allergy and Immunology, 21, 493-500. Blackwell Publishing
Pediatric Allergy and Immunology, 21, 3, pp. 493-500
Pediatric Allergy and Immunology, 21, 493-500
Pediatric Allergy and Immunology, 21(3), 493-500. Wiley

Contains fulltext : 89139.pdf (Publisher’s version ) (Closed access) Cystic fibrosis (CF) lung disease is characterized by chronic airway inflammation and recurrent infections, resulting in (ir)reversible structural lung changes and a progressive d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3b45fc9d76b3bdfb614bc54153d11432
https://pure.eur.nl/en/publications/d0709bfa-9d6c-4844-882a-254d4d1dcd11

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Growth monitoring to detect children with cystic fibrosis

Autor: Dommelen, P. van, Grote, F.K., Oostdijk, W., Muinck Keizer de, Schrama, S.M.P.F., Bouquet, J., Hendriks, J.J.E., Kouwenberg, J., Verkerk, P.H., Buuren, S. van, Wit, J.M.

Publikováno v: Hormone Research, 4, 72, 218-224

Background/Aims: Cystic fibrosis (CF) in infancy and childhood is often associated with failure to thrive (FTT). This would suggest that in countries without a newborn screening program for CF, FTT could be used as a clinical screening tool. The aim

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ca4ac65c4c5636a744a2969842d1faa2
http://resolver.tudelft.nl/uuid:c088ff7e-1989-4ecb-a71a-610c8da1b7ca

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Effects of a proton-pump inhibitor in cystic fibrosis

Autor: Tran, T.M., van den Neucker, A.M., Hendriks, J.J.E., Forget, Ph.

Publikováno v: Acta Paediatrica, 87(5), 553-558. Wiley

Department of Pediatrics, University Hospital of Maastricht, The Netherlands. Most children with cystic fibrosis (CF) show persisting steatorrhoea even when treated with pancreatic enzyme. As a low duodenal pH could be responsible for this persisting

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::9efe7130f25c19e6a30cdd695dc7913f
https://cris.maastrichtuniversity.nl/en/publications/a25db68b-5944-4c26-82e7-3f9ba0378ae9

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Akademický článek

Clinical outcome and meconium ileus in Dutch cystic fibrosis patients

Autor: Zwitserloot, A.M., Roukema, J., Bronsveld, I., Hendriks, J.J.E., Nuijsink, M., Pijnenburg, M.W., Rottier, B.L., Vreede, I., Merkus, P.

Publikováno v: In Paediatric Respiratory Reviews July 2013 14 Supplement 2:S70-S70

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